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Ò¹ò­¶ù(¶¹¸ç´ú·¢): ½ð±Ò+10, лл 2013-05-29 15:24:40
1 .     19(S)-hydroxyibogamine
C19H24N2O     ÏàËÆ¶È:94.7%
Journal of Natural Products          2002          65          669-672
Five New Iboga Alkaloids from Tabernaemontana corymbosa
Toh-Seok Kam and Kooi-Mow Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     ibogamine
    ÏàËÆ¶È:73.6%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     ibogamine
    ÏàËÆ¶È:73.6%
Qu¨ªmica Nova          2008          31          20-24
Chemical constituents from Tabernaemontana catharinensis root bark: a brief NMR review of indole alkaloids and in vitro cytotoxicity
Pereira, Paulo S¨¦rgio; França, Suzelei de Castro; Oliveira, Paulo Vinicius Anderson de; Breves, Camila Moniz de Souza; Pereira, Sarazete Izidia Vaz; Sampaio, Suely Vilela; Nomizo, Auro; Dias, Diones Aparecida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1-ethyl-1-methyl-1,2,3,4-tetrahydro-¦Â-carboline
C14H18N2     ÏàËÆ¶È:66.6%
Heterocycles          2003          59          691-705
A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent
Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     cleavamine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          1976          59          2711-2723
13C-NMR. Spectroscopy of Naturally Occuring Substances. XLII. Conformational analysis of quebrachamine-like indole alkaloids and related substances
Ernest Wenkert, Edward W. Hagaman, Nicole Kunesch, Nai-yi Wang and B¨¦la Zsadon
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     ibogamine
    ÏàËÆ¶È:63.1%
Helvetica Chimica Acta          2010          93          422-429
Two New Indole Alkaloids from Tabernaemontana hystrixSteud. (Apocynaceae)
Jucimar J. de Souza, Leda Mathias, Raimundo Braz-Filho and Ivo J. Curcino Vieira
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     14¦Â,15¦Â-20S-quebrachamine
C19H26N2O2     ÏàËÆ¶È:63.1%
Phytochemistry          2012          83          116-124
Alkaloids from Melodinus yunnanensis
Xiang-Hai Cai, Yan Li, Ya-Ping Liu, Xiao-Ning Li, Mei-Fen Bao, Xiao-Dong Luo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     nazlinine
    ÏàËÆ¶È:61.1%
Journal of Natural Products          1997          60          791-793
Reductive Pictet-Spengler Cyclization of Nitriles in the Presence of Tryptamine: Synthesis of Indolo[2, 3-a]quinolizidine, Nazlinine, and Elaeocarpidine
Khalid Diker, Khalid El Biach, Mich¨¨le Dö¨¦de Maindreville, and Jean L¨¦vy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     20-desethyl-(20-endo)-hydroxymethyl-11-demethoxyibogaine
C18H22N2O     ÏàËÆ¶È:61.1%
Natural Product Research          2006          20          758-765
Nature-inspired indolyl-2-azabicyclo[2.2.2]oct-7-ene derivatives as promising agents for the attenuation of withdrawal symptoms: synthesis of 20-desethyl-20-hydroxymethyl-11-demethoxyibogaine
D. Passarella; A. Barilli; S. M. N. Efange; E. Elisabetsky; M. B. Leal; G. Lesma; V. M. Linck; D. C. Mash; M. Martinelli; I. Peretto; A. Silvani; B. Danieli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     1-methyl-1-phenylsulfanyl-1,2,3,4-tetrahydro-¦Â-carboline
    ÏàËÆ¶È:61.1%
Heterocycles          2003          59          691-705
A Facile Synthesis of 1,1-Disubstituted 1,2,3,4-Tetrahydro-¦Â-carbolines via Trifluoroacetic Acid Catalyzed Pictet-Spengler Reaction Using Titanium (IV) Isopropoxide as an Imination Reagent
Yoshie Horiguchi,* Masayoshi Nakamura, Akiko Kida, Hirokazu Komada, Toshiaki Saitoh, and Takehiro Sano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

11 .     compound 10
C21H32N2O2Si     ÏàËÆ¶È:61.1%
Tetrahedron          1998          54          14845-14858
First total synthesis of 19S-hydroxytacamine, an indole alkaloid from Tabernaemontana eglandulosa, and of its C-19 stereoisomer, 19R-hydroxytacamine
Mauri Lounasmaa, David Din Belle, Arto Tolvanen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     compound 23
C22H32N2O2Si     ÏàËÆ¶È:61.1%
Tetrahedron          1998          54          14845-14858
First total synthesis of 19S-hydroxytacamine, an indole alkaloid from Tabernaemontana eglandulosa, and of its C-19 stereoisomer, 19R-hydroxytacamine
Mauri Lounasmaa, David Din Belle, Arto Tolvanen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     epiibogamine
    ÏàËÆ¶È:57.8%
Helvetica Chimica Acta          1976          59          2437-2442
13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids
Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

14 .     dehydrokoumidine
C19H20N2O     ÏàËÆ¶È:57.8%
Chemistry ¨C An Asian Journal          2011          6          166-173
Seven New Monoterpenoid Indole Alkaloids from Gelsemium elegans
Yousuke Yamada, Mariko Kitajima, Noriyuki Kogure, Sumphan Wongseripipatana, and Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (-)-Dihydrocorynanthenol
C19H26N2O     ÏàËÆ¶È:57.8%
European Journal of Organic Chemistry          2012                   398-408
Concise Total Synthesis of Dihydrocorynanthenol, Protoemetinol, Protoemetine, 3-epi-Protoemetinol and Emetine
Shuangzheng Lin, Luca Deiana, Abrehet Tseggai and Armando C¨®rdova
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (-)-nitraraine
C20H24N2O     ÏàËÆ¶È:57.8%
Heterocycles          2001          54          43-47
Cascading Single-step Stereoselective Construction of the ¦Á-Alloyohimbine Framework: A New Synthesis of (-)-Nitraraine
Hideki Sakagami and Kunio Ogasawara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

17 .     (-)-alloyohimbane
C19H24N2     ÏàËÆ¶È:57.8%
Heterocycles          2000          52          261-272
Application of Oxidative Desymmetrization of meso-Tetrahydrofurans: Syntheses of Functionalized Chiral Building Blocks and of (-)-Alloyohimbane
Akio Miyafuji, Katsuji Ito, and Tsutomu Katsuki*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     (3R,16R)-14,15-dihydroeburnamenin-19-one
C19H22N2O     ÏàËÆ¶È:57.8%
Tetrahedron          2004          60          3273-3282
Total syntheses of (−-vallesamidine and related Aspidosperma and Hunteria type indole alkaloids from the common intermediate
Hideo Tanino, Kazuhisa Fukuishi, Mina Ushiyama, Kunisuke Okada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (¡À)-cleavamine
    ÏàËÆ¶È:57.8%
Tetrahedron          2013          69          2534-2541
Synthesis of cleavamine-type indole alkaloids and their 5-nor derivatives by a ring-closing metathesis¨Cvinyl halide Heck cyclization strategy
M.-Lluïsa Bennasar, Daniel Sol¨¦, Ester Zulaica, Sandra Alonso
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

20 .     19-epi-heyneanine
    ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          2007          32          1296-1299
Study on chemical constituents in rhigome of Ervatamia hainanensis
LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

21 .     ¦Â-yohimbine
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1983          Vol 46          708-722
Aspidosperma de Guyane: Alcaloïdes des Graines de Aspidosperma oblongum
G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, H. Jacquemin, S. K. Kan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     ¦Â-yohimbine
    ÏàËÆ¶È:57.1%
Phytochemistry          1992          31          2031-2034
Alkaloid distribution in Malaysian Uncaria
Toh-Seok Kam, Kee-Huat Lee, Swee-Hock Goh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     compound 21
    ÏàËÆ¶È:56.5%
Journal of Heterocyclic Chemistry          2000          37          245-251
Synthesis of vinca alkaloids and related compounds part 94. Epimerization of compounds with aspidospermane and D-secoaspidospermane skeleton
György Kalaus, Lajos Szab¨®, J¨¢nos Éles, Csaba Sz¨¢ntay, Imre Juh¨¢sz, IstvÁn Greiner, J¨¢nos Brlik and M¨¢ria Kajt¨¢r-Peredy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     2-(2,3,4,9-tetrahydro-1H-¦Â-carbolin-1-yl)ethylamine
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1997          60          791-793
Reductive Pictet-Spengler Cyclization of Nitriles in the Presence of Tryptamine: Synthesis of Indolo[2, 3-a]quinolizidine, Nazlinine, and Elaeocarpidine
Khalid Diker, Khalid El Biach, Mich¨¨le Dö¨¦de Maindreville, and Jean L¨¦vy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

25 .     De-A,B-22-benzenesulphonyl-23,24-dinorcholestan-8-ol
    ÏàËÆ¶È:55.5%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

26 .     16-hydroxy-16,22-dihydroapparicine
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1984          Vol 47          835-838
16(S)-Hydroxy-16,22-dihydroapparicine, a New Alkaloid from the Leaves of Tabernaemontana dichotoma
P. Perera, T. A. van Beek, R. Verpoorte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

27 .     borrerine
    ÏàËÆ¶È:55.5%
Journal of Natural Products          1985          Vol 48          120-123
RMN du Carbone 13 des Alcaloïdes du Type Borr¨¦rine-Borr¨¦v¨¦rine-Isoborr¨¦v¨¦rine
F. Tillequin, M. Koch, A. Rabaron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

28 .     woodinine
C17H22N3Br     ÏàËÆ¶È:55.5%
Journal of Natural Products          1988          Vol 51          799
Alcaloïdes d'une Ascidie Neocaledonienne, Eudistoma fragum
C¨¦cile Debitus, Dominique Laurent, Mary Païs
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

29 .     compound 11
    ÏàËÆ¶È:55.5%
Helvetica Chimica Acta          1976          59          2254-2260
13C-NMR. Analysis of the Roxburghines
Lucio Merlini, Rosanna Mondelli, Gianluca Nasini, Felix W. Wehrli, Edward W. Hagaman and Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

30 .     corynantheol
    ÏàËÆ¶È:55.5%
Phytochemistry          1987          26          2839-2846
Alkaloids of Strychnos johnsonii
Georges Massiot,Philippe Th¨¦penier,Marie-Jos¨¦ Jacquier,Louisette Le Men-Olivier,Robert Verpoorte,Cl¨¦ment Delaude
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3Â¥2013-04-24 20:17:16
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